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  • 1960-1964  (4)
  • Chemistry  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 6 (1960), S. 171-172 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 1 (1961), S. 191-198 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Interfacial reactions between organosilane-treated fiberglass and styrene, and bond conditions in these and in polymerized ethylene oxide and epichlorhydrin-E-glass systems were investigated. The vinyl functionality of some alkenylsilanes showed little effect on the polymerization of styrene on E-glass. The polymerization of this aromatic monomer on vinyltrichlorosilane-reacted fiberglass did not result in interfacial bond formation. Sorption of water on organosilane-coated glass at different temperatures suggested that permeation of the adsorbate into the bulk of the substrate was determined by diffusive transfer of water molecules.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 47 (1964), S. 951-956 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crystals of 1,6-trans-dibromcyclodecane are monoclinic, a = 7,94, b =5,65, c = 12,78 A, β = 106° 47′, space group P2, lc. The unit cell contains two centrosymmetric molecules. The crystal structure has been determined by analysis of the three prin- cipal projections. The ring skeleton has the same conformation as that found in all previously studied cyclodecane compounds, with the substituents in (IIe, IIe) positions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 47 (1964), S. 1138-1147 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crystals of azacyclododecane hydrochloride (a = 13.77, b = 5.07, c = 9.67 Å, α = 109°26′, β = 90°22′, γ = 101°16′) and hydrobromide (a = 13.53, b = 5.19, c = 9.45 Å, α = 99°40′, β = 83°57′, γ = 98°28′) are isomorphous, space group P1, Z = 2. The conformation of the 12-membered ring has been established from three-dimensional X-ray analysis. It corresponds closely to the idealized model with 422-symmetry, containing 8 syn-clinal and 4 anti-periplanar partial conformations.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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